Holter Analysis Software (UDI 06974782940936)
Manufactured by Wuhan United Imaging Surgical Co., Ltd.
Device Regulatory Overview
The Holter Analysis Software (Model/Catalog Number: 88001269) is a medical device manufactured by Wuhan United Imaging Surgical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12050392 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 88001269
- Product Code / EMDN
- Z12050392
- Device Name
- uMH WS300
- Database Sync Date
- 2026-08-09 19:05:29
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Holter Analysis Software?
The registered manufacturer of record for Holter Analysis Software is Wuhan United Imaging Surgical Co., Ltd..
What is the Primary UDI-DI identifier for Holter Analysis Software?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974782940936.
What classification code is assigned to this device?
This device is registered under product classification code Z12050392.
Similar Classification Devices (Z12050392)
Other Devices by Wuhan United Imaging Surgical Co., Ltd.
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